STUGERON

This brand name is authorized in Brazil, Cyprus, Ecuador, Estonia, Ireland, Lithuania, Malta, Mexico, Romania, Singapore, South Africa, Spain, UK.

Active ingredients

The drug STUGERON contains one active pharmaceutical ingredient (API):

1
UNII 3DI2E1X18L - CINNARIZINE
 

Cinnarizine has been shown to be a non-competitive antagonist of the smooth muscle contractions caused by various vasoactive agents including histamine. Cinnarizine also acts on vascular smooth muscle by selectively inhibiting the calcium influx into depolarised cells, thereby reducing the availability of free Ca2+ ions for the induction and maintenance of contraction.

 
Read more about Cinnarizine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 STUGERON Tablet MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
N07CA02 Cinnarizine N Nervous system → N07 Other nervous system drugs → N07C Antivertigo preparations → N07CA Antivertigo preparations
Discover more medicines within N07CA02

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 514504601115316, 514504602111314
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 26.155-02-05
EE Ravimiamet 1008953
ES Centro de información online de medicamentos de la AEMPS 53025
GB Medicines & Healthcare Products Regulatory Agency 121347, 15693
IE Health Products Regulatory Authority 47368
LT Valstybinė vaistų kontrolės tarnyba 1012300, 1012913, 1067512
MT Medicines Authority MA018/02501
MX Comisión Federal para la Protección contra Riesgos Sanitarios 84564
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W10590001
SG Health Sciences Authority 01122P
ZA Health Products Regulatory Authority C/5.7/590, G/5.7.1/58

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